Description
We're seeking a passionate Clinical Research Associate (CRA) to join our team, playing a vital role in delivering high-quality clinical trials. You'll collaborate with investigative sites and cross-functional teams to ensure studies are conducted with excellence, compliance, and a patient focus.
Responsibilities
- Lead and execute site monitoring visits in accordance with GCP/ICH guidelines
- Build strong relationships with investigative sites to drive performance, recruitment, and engagement
- Ensure protocol compliance, data integrity, and high-quality study execution
- Proactively identify risks, resolve issues, and escalate when needed
- Track and manage study progress, including regulatory approvals, enrollment, and data quality
- Maintain accurate documentation and contribute to inspection readiness
- Collaborate with cross-functional teams to ensure successful study delivery
Requirements
- Bachelor's degree in life sciences, healthcare, or related field (or equivalent experience)
- 1.5+ years of on-site monitoring experience
- Solid understanding of GCP, ICH, and regulatory requirements
- Strong communication, problem-solving, and organizational skills
- Ability to manage multiple priorities in a fast-paced environment
Benefits
- Make a direct impact on advancing clinical research and improving patient outcomes
- Work alongside experienced, collaborative teams
- Opportunities for growth and career development
- Dynamic, fast-paced environment where your contributions matter
The potential base pay range for this role is $90,200.00 - $175,100.00 per year.